The Cost-Effectiveness of Personalized Genetic Medicine: The case of genetic testing in neonatal diabetes

OBJECTIVE: Neonatal diabetes mellitus is a rare form of diabetes diagnosed in infancy. Nearly half of patients with permanent neonatal diabetes have mutations in the genes for the ATP-sensitive potassium channel (KCNJ11 and ABCC8) that allow switching from insulin to sulfonylurea therapy. Although t...

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Detalles Bibliográficos
Autores principales: Greeley, Siri Atma W., John, Priya M., Winn, Aaron N., Ornelas, Joseph, Lipton, Rebecca B., Philipson, Louis H., Bell, Graeme I., Huang, Elbert S.
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2011
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041194/
https://www.ncbi.nlm.nih.gov/pubmed/21273495
http://dx.doi.org/10.2337/dc10-1616

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041194/
https://www.ncbi.nlm.nih.gov/pubmed/21273495
http://dx.doi.org/10.2337/dc10-1616

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